Evidence map›Paper›PMID 24873988›Full record

ArticleIntegrative biology : quantitative biosciences from nano to macro2014

Sonic hedgehog and neurotrophin-3 increase oligodendrocyte numbers and myelination after spinal cord injury.

Aline M Thomas, Stephanie K Seidlits, Ashley G Goodman, Todor V Kukushliev, Donna M Hassani, Brian J Cummings, Aileen J Anderson, Lonnie D Shea

Abstract read
In one paragraph

Article in Integrative biology : quantitative biosciences from nano to macro, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed, 1 pooled it
3.9field-weighted citation impact, top 6% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

41 citing papers in PubMed, 1 synthesis or guideline pooled it, 71 citations in OpenAlex.

  1. Pooled it
  2. Review
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  8. Review
  9. Sonic Hedgehog modulates the inflammatory response and improves functional recovery after spinal cord injury in a thoracic contusion-compression model.European spine journal : official publication of the European Spine Society, the European Spinal Deformity Society, and the European Section of the Cervical Spine Research Society · 2021
    Article
  10. Review
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  17. Regenerative Therapies for Spinal Cord Injury.Tissue engineering. Part B, Reviews · 2019
    Review
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 1 country.

Aline M Thomas *Department of Biomedical Engineering, McCormick School of Engineering, Northwestern University, Evanston, IL, USA.
Stephanie K Seidlits *Department of Chemical and Biological Engineering, McCormick School of Engineering, Northwestern University, Evanston, IL, USA.
Ashley G GoodmanDepartment of Chemical and Biological Engineering, McCormick School of Engineering, Northwestern University, Evanston, IL, USA.
Todor V KukushlievDepartment of Chemical and Biological Engineering, McCormick School of Engineering, Northwestern University, Evanston, IL, USA.
Donna M HassaniDepartment of Psychology, Weinberg College of Arts and Sciences, Northwestern University, Evanston, IL, USA.
Brian J CummingsDepartment of Physical Medicine and Rehabilitation, University of California, Irvine, CA, USA.
Aileen J AndersonDepartment of Physical Medicine and Rehabilitation, University of California, Irvine, CA, USA.
Lonnie D SheaDepartment of Chemical and Biological Engineering, McCormick School of Engineering, Northwestern University, Evanston, IL, USA.
Northwestern University · USUniversity of California, Irvine · US

Funding

Tumor Environment and Metastasis (TEAM) Research ProgramP30CA060553 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Daniela E Matei · 1993 to 2026
$153.9M
Regenerative Scaffold Technologies for CNS and DiabetesR01EB003806 · NIBIB · NORTHWESTERN UNIVERSITY AT CHICAGO · PI STUPP, SAMUEL I · 2004 to 2015
$10.7M
Mentoring For Success: Developing Fundamental Skills For Biomedical ResearchR25GM079300 · NIGMS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI MCGEE, RICHARD · 2007 to 2020
$6.6M
Controlled Release Scaffolds for Nerve RegenerationR01EB005678 · NIBIB · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ANDERSON, AILEEN J, SHEA, LONNIE D · 2007 to 2018
$6.0M
An in vivo metastasis sensorR01CA173745 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI BACKMAN, VADIM, SHEA, LONNIE D · 2012 to 2016
$4.2M
Parallel gene delivery from spinal cord bridgesR21EB006520 · NIBIB · NORTHWESTERN UNIVERSITY · PI SHEA, LONNIE D · 2007 to 2008
$383k
Directed Differentiation of Stem Cell Transplants into Myelinating GliaF32NS081961 · NINDS · NORTHWESTERN UNIVERSITY · PI SEIDLITS, STEPHANIE KRISTIN · 2012 to 2014
$68k
NCI NIH HHS P30 CA060553NCI NIH HHS R01 CA173745NIBIB NIH HHS R01 EB003806NIBIB NIH HHS R01 EB005678NIBIB NIH HHS R21 EB006520NIGMS NIH HHS R25 GM079300NINDS NIH HHS F32 NS081961
6 · The paper itself

Abstract

Spinal cord injury (SCI) results in loss of sensory and motor function below the level of injury and has limited available therapies. Multiple channel bridges have been investigated as a means to create a permissive environment for regeneration, with channels supporting axonal growth through the injury. Bridges support robust axon growth and myelination. Here, we investigated the cell types that myelinate axons in the bridges and whether over-expression of trophic factors can enhance myelination. Lentivirus encoding for neurotrophin-3 (NT3), sonic hedgehog (SHH) and the combination of these factors was delivered from bridges implanted into a lateral hemisection defect at T9/T10 in mice, and the response of endogenous progenitor cells within the spinal cord was investigated. Relative to control, the localized, sustained expression of these factors significantly increased growth of regenerating axons into the bridge and enhanced axon myelination 8 weeks after injury. SHH decreased the number of Sox2(+) cells and increased the number of Olig2(+) cells, whereas NT3 alone or in combination with SHH enhanced the numbers of GFAP(+) and Olig2(+) cells relative to control. For delivery of lentivirus encoding for either factor, we identified cells at various stages of differentiation along the oligodendrocyte lineage (e.g., O4(+), GalC(+)). Expression of NT3 enhanced myelination primarily by infiltrating Schwann cells, whereas SHH over-expression substantially increased myelination by oligodendrocytes. These studies further establish biomaterial-mediated gene delivery as a promising tool to direct activation and differentiation of endogenous progenitor cells for applications in regenerative medicine.

Indexed as

AnimalsAxonsCell DifferentiationFemaleGenetic TherapyHedgehog ProteinsImmunohistochemistryMiceMice, Inbred C57BLNeurotrophin 3OligodendrogliaRegenerative MedicineSpinal Cord InjuriesStem CellsHedgehog ProteinsNeurotrophin 3Shh protein, mouse

Identifiers

PMID24873988
PMCPMC4086750
OpenAlexW2049916693

What OpenQuestion holds

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Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.